| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4632987
Max Phase: Preclinical
Molecular Formula: C15H10BrNO5
Molecular Weight: 364.15
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: O=C(/C=C/c1cccc(Br)c1)c1cc(O)c(O)c([N+](=O)[O-])c1
Standard InChI: InChI=1S/C15H10BrNO5/c16-11-3-1-2-9(6-11)4-5-13(18)10-7-12(17(21)22)15(20)14(19)8-10/h1-8,19-20H/b5-4+
Standard InChI Key: FOHHARPNBZPXNS-SNAWJCMRSA-N
Associated Targets(Human)
Catechol O-methyltransferase 404 Activities
Monoamine oxidase B 8835 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Monoamine oxidase A 11911 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 364.15 | Molecular Weight (Monoisotopic): 362.9742 | AlogP: 3.66 | #Rotatable Bonds: 4 |
| Polar Surface Area: 100.67 | Molecular Species: ACID | HBA: 5 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 5.61 | CX Basic pKa: | CX LogP: 3.99 | CX LogD: 2.41 |
| Aromatic Rings: 2 | Heavy Atoms: 22 | QED Weighted: 0.28 | Np Likeness Score: -0.43 |
References
| 1. Hitge R, Smit S, Petzer A, Petzer JP.. (2020) Evaluation of nitrocatechol chalcone and pyrazoline derivatives as inhibitors of catechol-O-methyltransferase and monoamine oxidase., 30 (12): [PMID:32299731] [10.1016/j.bmcl.2020.127188] |
Source
Source(1):